NDUFA8 potentially rescues Wolbachia-induced cytoplasmic incompatibility in Laodelphax striatellus.

The endosymbiont Wolbachia manipulates host reproduction by several strategies, one of the most important of which is cytoplasmic incompatibility (CI). CI can be rescued when Wolbachia-infected males mate with females infected with the same Wolbachia strain. However, the potential rescue mechanism of CI in the small brown planthopper Laodelphax striatellus is unclear. In this study, comparative transcriptome analysis was applied to explore the effect of Wolbachia on L. striatellus eggs. A total of 1387 differentially expressed genes were identified. RNA interference of 7 Wolbachia-upregulated key planthopper genes reduced egg reproduction, suggesting that Wolbachia might improve fecundity in L. striatellus by affecting these 7 genes. Suppressing the expression of another upregulated gene, NDUFA8 (encoding NADH dehydrogenase [ubiquinone] 1 α subcomplex subunit 8-like) by RNA interference significantly increased the mortality of early embryos without affecting the number of deposited eggs. Wolbachia infection upregulated the mRNA level of NDUFA8, and dsNDUFA8 treatment of Wolbachia-infected females recreated CI-like symptoms, suggesting that NDUFA8 is associated with the rescue phenotype. Because all L. striatellus populations worldwide are infected with Wolbachia, NDUFA8 is a potential pest control target.

Electrochemical transformation of limestone into calcium hydroxide and valuable carbonaceous products for decarbonizing cement production.

The cement industry is one of the largest contributors to global CO2 emissions, which has been paid more attention to the research on converting the CO2 released by the cement production process. It is extremely challenging to decarbonize the cement industry, as most CO2 emissions result from the calcination of limestone (CaCO3) into CaO and CO2. In this work, we demonstrate an in situ electrochemical process that transforms CaCO3 into portlandite (Ca(OH)2, a key Portland cement precursor) and valuable carbonaceous products, which integrates electrochemical water splitting and CO2 reduction reaction with the chemical decomposition of CaCO3. With different metal catalyst electrodes (like Au, Ag, In, Cu, and Cu nanowires electrodes), we have achieved various valuable carbonaceous products, such as CO, formate, methane, ethylene, and ethane during the electrochemical CO2 process. Our work demonstrates a proof of concept for green and sustainable cement production.

Selective electrochemical reduction of carbon dioxide to ethylene on a copper hydroxide nitrate nanostructure electrode.

Electrochemical carbon dioxide reduction (CO2 RR) is a promising technology to convert CO2 into valuable carbon-based fuels and chemicals. Copper (Cu) is a unique catalyst for this reaction as it yields substantial hydrocarbon products, but still suffers from low selectivity in aqueous solution. Here, we present a nanostructure Cu@Cu2(OH)3NO3 electrode using a facile molten salt decomposition method (MSDM). Both XPS and XRD data indicate that Cu2(OH)3NO3 is converted into metallic Cu when employed in CO2 electroreduction in KHCO3 solution, leaving abundant defects on the dendritic rough surface. Benefiting from the defects and rough surface, this electrode exhibited a high selectivity for C2H4 production with a faradaic efficiency (FE) of 31.80% and a high stability for 20 h.

Activating basal plane in NiFe layered double hydroxide by Mn2+ doping for efficient and durable oxygen evolution reaction.

Foreign metal ions with reducing ability were doped into NiFe layered double hydroxides (NiFe-LDHs) to activate the basal plane in NiFe-LDHs for oxygen evolution reaction (OER). Mn2+-Doped NiFe-LDH array electrode yields a low onset potential of 1.41 V and exhibits outstanding stability. The study herein illustrates a new dimension of electronic structure regulation and promises further optimization of highly efficient electrocatalysts.